Heparin is a promising agent for the treatment of endometriosis-associated fibrosis
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This study investigated heparin as a potential treatment for endometriosis-associated fibrosis, finding it to be a promising agent.
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Abstract
ObjectiveTo assess the use of heparin for the medical treatment of endometriosis-associated fibrosis.DesignThe effects of heparin on the endometriotic stromal cells (ECSCs)-mediated contractility were investigated.SettingResearch laboratory at a medical school.Patient(s)Endometriotic tissues from nine patients were used.Intervention(s)Endometriotic stromal cells were cultured three dimensionally in the presence of heparin.Main outcome measure(s)The contractility of ECSCs was assessed by collagen gel contraction assay. Heparin-induced morphological changes of ECSCs were evaluated by laser scanning microscopy. The expression of contractility-related molecules in ECSCs was examined by Western blot analysis.Result(s)In the presence of 10% fetal bovine serum, treated ECSCs showed significant collagen gel contractility (75.9% decrease in surface area after 48 hour vs. 0 hour controls). Endometriotic stromal cell-mediated gel contraction was significantly attenuated in the presence of heparin in a dose-dependent manner (55.7% reduction of the gel contraction at a concentration of 100 microg/mL of heparin sodium versus untreated controls after 48 hours). Heparin suppressed the ECSC attachment to collagen fibers. The expression of alpha-smooth muscle actin, Ras homology (Rho) A, Rho-associated coiled-coil-forming protein kinase (ROCK)-I, and ROCK-II was down-regulated by heparin administration.Conclusion(s)The present study suggests that heparin is a promising agent for the treatment of endometriosis-associated fibrosis. The inhibition of myofibroblastic differentiation, the attenuation of attachment to collagen fibers, and the suppression of Rho-ROCK-mediated pathway activation in ECSCs are involved in the action mechanisms of heparin.
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Cited by (14)
- Endometriosis-associated Pain: Mechanism, Neuroimmune Signature, and Translational Precision Strategies 2026
- The role of fibrosis in endometriosis: a systematic review 2024
- Endometriosis, the Silent Disease: Molecular Targets, Active Principles, and Drug Delivery Systems 2022
- New Therapeutics in Endometriosis: A Review of Hormonal, Non-Hormonal, and Non-Coding RNA Treatments 2021
- Pharmaceuticals targeting signaling pathways of endometriosis as potential new medical treatment: A review 2021
- Chemokine expression profiles of ovarian endometriotic stromal cells in three-dimensional culture 2020
- Revealing the enigma of coagulation in endometriosis: the risk of thrombosis and the role of antithrombotic treatment 2020
- Biological characteristics of endometriotic mesenchymal stem cells isolated from ectopic lesions of patients with endometriosis 2020
- β-catenin signaling inhibitors ICG-001 and C-82 improve fibrosis in preclinical models of endometriosis 2019
- Platelets drive smooth muscle metaplasia and fibrogenesis in endometriosis through epithelial–mesenchymal transition and fibroblast-to-myofibroblast transdifferentiation 2016
- Dysregulated cell mechanical properties of endometrial stromal cells from endometriosis patients. 2014
- Potential New Drugs for Endometriosis: Experimental Evidence 2014
- Fasudil Inhibits the Proliferation and Contractility and Induces Cell Cycle Arrest and Apoptosis of Human Endometriotic Stromal Cells: A Promising Agent for the Treatment of Endometriosis 2011
- Mevalonate-Ras Homology (Rho)/Rho-Associated Coiled-Coil-Forming Protein Kinase (ROCK)-Mediated Signaling Pathway as a Therapeutic Target for the Treatment of Endometriosis-Associated Fibrosis 2010
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- europepmc
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